Phase
Condition
Stimulant Use Disorder
Treatment
Placebo (for d-amphetamine)
Contingency management
d-amphetamine
Clinical Study ID
Ages 18-60 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
be between 18 and 60 years of age
meet Diagnostic and Statistical Manual V (DSM-5) criteria for current cocaine usedisorder of at least moderate severity (≥ 4 symptoms)
have at least 1 cocaine positive urine sample during the baseline screening period
be in acceptable health on the basis of interview, medical history and physicalexam, per the judgment of our study physician
be able to understand the consent form and provide written informed consent
be able to provide the names of at least 2 persons who can generally locate theirwhereabouts.
if female, agree to use an acceptable method of birth control during study (surgicalsterilization, approved hormonal contraceptives, barrier methods with spermicide, orintrauterine device).
Exclusion
Exclusion Criteria:
current DSM-5 diagnosis for substance use disorder of least moderate severity (≥ 4symptoms), other than cocaine, nicotine, marijuana, or alcohol
Physical dependence on alcohol requiring medically supervised detoxification, in thejudgment of the study physician
current amphetamine use (by self-report in past 30 days or positive urine drugscreen), more than 50 lifetime uses of amphetamine, or history of DSM-5 AmphetamineUse Disorder
a current DSM-5 axis I psychiatric disorder or neurological disease or disorderrequiring ongoing treatment and/or making study participation unsafe
significant current suicidal or homicidal ideation
medical conditions contraindicating d-amphetamine (e.g., significant cardiovasculardisease, liver or kidney disease, seizure disorder, hypotension or hypertension)
taking medications known to have effects on the central nervous system or that couldcause significant drug interactions with d-amphetamine (e.g., clonidine, prazosin)
having conditions of probation or parole requiring reports of drug use to officersof the court
impending incarceration
pregnant or nursing for female patients
inability to read, write, or speak English
Additional Exclusion Criteria for the functional magnetic resonance (fMRI) Sub-Study (in addition to all listed criteria above for the Main Treatment Study):
body mass index (BMI) >30, as this may be incompatible with the magnetic resonancescanner gantry
any retained metals in the body, including implants and metallic substances (e.g.aneurysm clips, retained metal particles in metal workers, magnetic dental implants,ferromagnetic ocular implants, iron-based facial tattoos), as this may cause adverseeffects to participants and interfere with data collection in the MR magnetic field
inability to tolerate small, enclosed spaces (such as the magnetic resonance scannerbore)
Study Design
Study Description
Connect with a study center
University of Illinois at Chicago
Chicago, Illinois 60607
United StatesSite Not Available
The University of Texas Health Science Center at Houston
Houston, Texas 77054
United StatesSite Not Available
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